Canonical Allele Identifier: CA1427629849
Gene:

Linked Data

dbSNP Id: rs1715476665

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931522G>A , CM000665.2:g.187931522G>A GRCh38
NC_000003.11:g.187649310G>A , CM000665.1:g.187649310G>A GRCh37
NC_000003.10:g.189132004G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1392C>T